Linked Data
ClinVar Variation Id:
2790245
ClinVar RCV Id:
RCV003669758
gnomAD v4:
10-49530699-CTGAA-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.49530702_49530705del , CM000672.2:g.49530702_49530705del | GRCh38 |
| NC_000010.10:g.50738748_50738751del , CM000672.1:g.50738748_50738751del | GRCh37 |
| NC_000010.9:g.50408754_50408757del | NCBI36 |
| NG_009442.1:g.13399_13402del , LRG_465:g.13399_13402del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000355832.10:c.543+17_543+20del MANE Select | ENSP00000348089.5:n.543+17_543+20del | |
| ENST00000447839.7:c.543+17_543+20del MANE Plus Clinical | ENSP00000387966.2:n.543+17_543+20del | |
| ENST00000679596.1:c.*172+1840_*172+1843del | ENSP00000504862.1:n.*172+1840_*172+1843de... | |
| ENST00000679811.1:n.626+17_626+20del | ||
| ENST00000680107.1:c.543+17_543+20del | ENSP00000505909.1:n.543+17_543+20del | |
| ENST00000680233.1:n.636+17_636+20del | ||
| ENST00000681632.1:n.621+17_621+20del | ||
| ENST00000681659.1:c.543+17_543+20del | ENSP00000505631.1:n.543+17_543+20del | |
| ENST00000355832.9:c.543+17_543+20del | ENSP00000348089.5:n.543+17_543+20del | |
| ENST00000447839.6:c.543+17_543+20del | ENSP00000387966.2:n.543+17_543+20del | |
| ENST00000479652.1:n.18+17_18+20del | ||
| ENST00000515869.1:c.543+17_543+20del | ENSP00000423550.1:n.543+17_543+20del | |
| NM_000124.3:c.543+17_543+20del | NP_000115.1:n.543+17_543+20del | |
| NM_001277058.1:c.543+17_543+20del | NP_001263987.1:n.543+17_543+20del | |
| NM_001277059.1:c.543+17_543+20del | NP_001263988.1:n.543+17_543+20del | |
| NM_001346440.1:c.543+17_543+20del | NP_001333369.1:n.543+17_543+20del | |
| NM_000124.4:c.543+17_543+20del MANE Select | NP_000115.1:n.543+17_543+20del | |
| NM_001277058.2:c.543+17_543+20del MANE Plus Clinical | NP_001263987.1:n.543+17_543+20del | |
| NM_001277059.2:c.543+17_543+20del | NP_001263988.1:n.543+17_543+20del | |
| NM_001346440.2:c.543+17_543+20del | NP_001333369.1:n.543+17_543+20del |